A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628996



Internal ID21821043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78201867..78201867hg38UCSC Ensembl
chr16:78235764..78235764hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085669
Supporting Variants
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628996
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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